A citation-based method for searching scientific literature

Gary Marchant, Mark Barnes, James P Evans, Bonnie LeRoy, Susan M Wolf. J Law Med Ethics 2020
Times Cited: 12







List of co-cited articles
28 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity




The law of incidental findings in human subjects research: establishing researchers' duties.
Susan M Wolf, Jordan Paradise, Charlisse Caga-anan. J Law Med Ethics 2008
72
25

How Can Law and Policy Advance Quality in Genomic Analysis and Interpretation for Clinical Care?
Barbara J Evans, Gail Javitt, Ralph Hall, Megan Robertson, Pilar Ossorio, Susan M Wolf, Thomas Morgan, Ellen Wright Clayton. J Law Med Ethics 2020
6
50

The law of genetic privacy: applications, implications, and limitations.
Ellen Wright Clayton, Barbara J Evans, James W Hazel, Mark A Rothstein. J Law Biosci 2019
35
25

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
25

Is there a duty to reinterpret genetic data? The ethical dimensions.
Paul S Appelbaum, Erik Parens, Sara M Berger, Wendy K Chung, Wylie Burke. Genet Med 2020
14
25


Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines.
Wylie Burke, Ellen Wright Clayton, Susan M Wolf, Susan A Berry, Barbara J Evans, James P Evans, Ralph Hall, Diane Korngiebel, Anne-Marie Laberge, Bonnie S LeRoy,[...]. Genet Med 2019
6
33

Integrating Rules for Genomic Research, Clinical Care, Public Health Screening and DTC Testing: Creating Translational Law for Translational Genomics.
Susan M Wolf, Pilar N Ossorio, Susan A Berry, Henry T Greely, Amy L McGuire, Michelle A Penny, Sharon F Terry. J Law Med Ethics 2020
7
28

Key Expert Stakeholder Perceptions of the Law of Genomics: Identified Problems and Potential Solutions.
Fook Yee Cheung, Lauren Clatch, Susan M Wolf, Ellen Wright Clayton, Frances Lawrenz. J Law Med Ethics 2020
2
100

Regulatory changes raise troubling questions for genomic testing.
Barbara J Evans, Michael O Dorschner, Wylie Burke, Gail P Jarvik. Genet Med 2014
18
16

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
842
16

The role of patient advocacy organizations in shaping genomic science.
Pei P Koay, Richard R Sharp. Annu Rev Genomics Hum Genet 2013
24
16

The historical foundations of the research-practice distinction in bioethics.
Tom L Beauchamp, Yashar Saghai. Theor Med Bioeth 2012
27
16


ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
16



Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG).
Joshua L Deignan, Wendy K Chung, Hutton M Kearney, Kristin G Monaghan, Catherine W Rehder, Elizabeth C Chao. Genet Med 2019
40
16

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics.
Daniele Carrieri, Heidi C Howard, Caroline Benjamin, Angus J Clarke, Sandi Dheensa, Shane Doheny, Naomi Hawkins, Tanya F Halbersma-Konings, Leigh Jackson, Hülya Kayserili,[...]. Eur J Hum Genet 2019
35
16

Physicians' duty to recontact and update genetic advice.
Yvonne A Stevens, Grant D Senner, Gary E Marchant. Per Med 2017
10
20

Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG).
Karen L David, Robert G Best, Leslie Manace Brenman, Lynn Bush, Joshua L Deignan, David Flannery, Jodi D Hoffman, Ingrid Holm, David T Miller, James O'Leary,[...]. Genet Med 2019
46
16

Letter: Relearning the 3 R's? Reinterpretation, recontact, and return of genetic variants.
Bartha Maria Knoppers, Adrian Thorogood, Ma'n H Zawati. Genet Med 2019
6
33

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.
Laura M Amendola, Gail P Jarvik, Michael C Leo, Heather M McLaughlin, Yassmine Akkari, Michelle D Amaral, Jonathan S Berg, Sawona Biswas, Kevin M Bowling, Laura K Conlin,[...]. Am J Hum Genet 2016
77
16


Return of individual genomic research results: are laws and policies keeping step?
Adrian Thorogood, Gratien Dalpé, Bartha Maria Knoppers. Eur J Hum Genet 2019
37
16

The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.
Yvonne Bombard, Kyle B Brothers, Sara Fitzgerald-Butt, Nanibaa' A Garrison, Leila Jamal, Cynthia A James, Gail P Jarvik, Jennifer B McCormick, Tanya N Nelson, Kelly E Ormond,[...]. Am J Hum Genet 2019
49
16

Unregulated Health Research Using Mobile Devices: Ethical Considerations and Policy Recommendations.
Mark A Rothstein, John T Wilbanks, Laura M Beskow, Kathleen M Brelsford, Kyle B Brothers, Megan Doerr, Barbara J Evans, Catherine M Hammack-Aviran, Michelle L McGowan, Stacey A Tovino. J Law Med Ethics 2020
15
8

Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
469
8

Medicine. Reestablishing the researcher-patient compact.
Isaac S Kohane, Kenneth D Mandl, Patrick L Taylor, Ingrid A Holm, Daniel J Nigrin, Louis M Kunkel. Science 2007
100
8

Self-guided management of exome and whole-genome sequencing results: changing the results return model.
Joon-Ho Yu, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Genet Med 2013
58
8

Offering individual genetic research results: context matters.
Laura M Beskow, Wylie Burke. Sci Transl Med 2010
133
8

Managing incidental genomic findings: legal obligations of clinicians.
Ellen Wright Clayton, Susanne Haga, Patricia Kuszler, Emily Bane, Krysta Shutske, Wylie Burke. Genet Med 2013
44
8

Biomedical Big Data: New Models of Control Over Access, Use and Governance.
Effy Vayena, Alessandro Blasimme. J Bioeth Inq 2017
31
8

Research led by participants: a new social contract for a new kind of research.
Effy Vayena, Roger Brownsword, Sarah Jane Edwards, Bastian Greshake, Jeffrey P Kahn, Navjoyt Ladher, Jonathan Montgomery, Daniel O'Connor, Onora O'Neill, Martin P Richards,[...]. J Med Ethics 2016
35
8

What does the duty to warn require?
Seema K Shah, Sara Chandros Hull, Michael A Spinner, Benjamin E Berkman, Lauren A Sanchez, Ruquyyah Abdul-Karim, Amy P Hsu, Reginald Claypool, Steven M Holland. Am J Bioeth 2013
13
8

Ethics. Incidental findings in brain imaging research.
Judy Illes, Matthew P Kirschen, Emmeline Edwards, L R Stanford, Peter Bandettini, Mildred K Cho, Paul J Ford, Gary H Glover, Jennifer Kulynych, Ruth Macklin,[...]. Science 2006
152
8

Citizen Science on Your Smartphone: An ELSI Research Agenda.
Mark A Rothstein, John T Wilbanks, Kyle B Brothers. J Law Med Ethics 2015
24
8

Web-based, participant-driven studies yield novel genetic associations for common traits.
Nicholas Eriksson, J Michael Macpherson, Joyce Y Tung, Lawrence S Hon, Brian Naughton, Serge Saxonov, Linda Avey, Anne Wojcicki, Itsik Pe'er, Joanna Mountain. PLoS Genet 2010
277
8



Is community-based participatory research possible?
Daniel S Blumenthal. Am J Prev Med 2011
48
8

Information access. Raw personal data: providing access.
Jeantine E Lunshof, George M Church, Barbara Prainsack. Science 2014
34
8

Incidental findings in human subjects research: what do investigators owe research participants?
Franklin G Miller, Michelle M Mello, Steven Joffe. J Law Med Ethics 2008
71
8

Incidental findings and ancillary-care obligations.
Henry S Richardson. J Law Med Ethics 2008
57
8



Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years.
Anne Andermann, Ingeborg Blancquaert, Sylvie Beauchamp, Véronique Déry. Bull World Health Organ 2008
431
8

Knowledge integration at the center of genomic medicine.
Muin J Khoury, Marta Gwinn, W David Dotson, Sheri D Schully. Genet Med 2012
19
8


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.